首页> 外文期刊>The Analyst: The Analytical Journal of the Royal Society of Chemistry: A Monthly International Publication Dealing with All Branches of Analytical Chemistry >A gold nanorods-based fluorescent biosensor for the detection of hepatitis B virus DNA based on fluorescence resonance energy transfer
【24h】

A gold nanorods-based fluorescent biosensor for the detection of hepatitis B virus DNA based on fluorescence resonance energy transfer

机译:一种基于金纳米棒的荧光生物传感器,用于基于荧光共振能量转移的乙型肝炎病毒DNA检测

获取原文
获取原文并翻译 | 示例
           

摘要

In this study, we designed a fluorescence resonance energy transfer system containing gold nanorods (AuNRs) and fluorescein (FAM) for the detection of hepatitis B virus DNA sequences. AuNRs were synthesized according to the seed-mediated surfactant-directed approach, and the surface of the AuNRs was wrapped with a thin layer of cetyltrimethylammonium bromide (CTAB), resulting in the AuNRs being positively charged. When FAM-tagged single-stranded DNA (FAM-ssDNA) was added into the AuNRs suspension, it was adsorbed onto the surface of the positively charged AuNRs and formed a FAM-ssDNA-CTAB-AuNRs ternary complex, the resulting structure led to a fluorescence resonance energy transfer (FRET) process from FAM to AuNRs and the fluorescence intensity of FAM was consequently quenched. When complementary target DNA was added to the FAM-ssDNA-CTAB-AuNRs complex solution, a further decrease in fluorescence intensity was observed because of an increased FRET efficiency. Under optimal conditions, the decline of the fluorescence intensity of FAM (ΔF) was linear with the concentration of the complementary DNA from 0.045 to 6.0 nmol L~(-1) and the detection limit was as low as 15 pmol L~(-1) (signaloise ratio of 3). When this fluorescent DNA sensor was used to detect the polymerase chain reaction product of hepatitis B virus gene extracted from a positive real sample, a positive response was obtained. Impressively, the biosensor exhibits good selectivity, even for single-mismatched DNA detection.
机译:在这项研究中,我们设计了一种包含金纳米棒(AuNRs)和荧光素(FAM)的荧光共振能量转移系统,用于检测乙型肝炎病毒DNA序列。根据种子介导的表面活性剂定向方法合成AuNRs,并用十六烷基三甲基溴化铵(CTAB)薄层包裹AuNRs的表面,使AuNRs带正电。当将带有FAM标签的单链DNA(FAM-ssDNA)添加到AuNRs悬浮液中时,它会吸附到带正电荷的AuNRs的表面上,并形成FAM-ssDNA-CTAB-AuNRs三元复合物,从而导致从FAM到AuNRs的荧光共振能量转移(FRET)过程和FAM的荧光强度因此被淬灭。当将互补的目标DNA添加到FAM-ssDNA-CTAB-AuNRs复合溶液中时,由于FRET效率提高,荧光强度进一步降低。在最佳条件下,FAM的荧光强度(ΔF)的下降与互补DNA的浓度从0.045至6.0 nmol L〜(-1)呈线性关系,检出限低至15 pmol L〜(-1) )(信噪比为3)。当使用该荧光DNA传感器检测从阳性真实样品中提取的乙型肝炎病毒基因的聚合酶链反应产物时,获得了阳性反应。令人印象深刻的是,即使对于单次不匹配的DNA检测,生物传感器也具有良好的选择性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号